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Published on: August 1, 2018
Celiac Disease and Portal Hypertension: A Causal Association or Just a Coincidence?
Amit Tanwar1, Gaurav K Gupta1, Virender Chauhan1
1Department of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Insights
Celiac disease (CD) is prevalent in patients with portal hypertension (PHT), particularly in cryptogenic liver disease and noncirrhotic PHT. Screening for CD is recommended in liver disease patients due to its higher likelihood.
Area of Science:
- Gastroenterology
- Hepatology
- Immunology
Background:
- Celiac disease (CD) has been anecdotally linked to portal hypertension (PHT).
- The etiological association between CD and PHT remains unproven.
- This study investigates the prevalence of CD in PHT patients across various etiologies.
Purpose of the Study:
- To determine the prevalence of celiac disease (CD) in patients diagnosed with portal hypertension (PHT).
- To explore the association between CD and different causes of PHT, including chronic liver disease (CLD) and noncirrhotic PHT (NCPHT).
Main Methods:
- A prospective observational study was conducted from June 2017 to December 2018.
- Patients with PHT (CLD and NCPHT) were screened for CD using IgA anti-tTG antibody tests.
- Serology-positive patients underwent duodenal biopsy for confirmation.
Main Results:
- Out of 464 PHT patients, 29 were diagnosed with CD.
- CD prevalence was 4.5% in chronic liver disease (CLD) patients and 14.6% in noncirrhotic PHT (NCPHT) patients.
- CD was notably found in patients with cryptogenic CLD (cCLD) and noncirrhotic portal fibrosis (NCPF).
Conclusions:
- Celiac disease (CD) is common in patients with portal hypertension (PHT) of diverse etiologies.
- The prevalence of CD is significantly higher in liver disease patients compared to the general population.
- Routine screening for CD is advised in patients with PHT, especially those with cryptogenic CLD, NCPHT, and autoimmune hepatitis.
Introduction:
Celiac disease (CD) has been linked to portal hypertension (PHT) of varied etiology, but the causality association has never been proved. We aim to study the prevalence of CD in patients of PHT of different etiology.
Methods:
A prospective observational study was conducted from June 2017 to December 2018 involving all the cases of PHT of varied etiology. Consecutive patients of PHT with chronic liver disease (CLD) of defined etiology like ethanol, viral hepatitis (B or C), Budd-Chiari syndrome (BCS), autoimmune-related cirrhosis, and cryptogenic CLD (cCLD) (group A) and those with noncirrhotic PHT (NCPHT), which included noncirrhotic portal fibrosis (NCPF) and extrahepatic portal vein obstruction (EHPVO) (group B), were screened for CD by IgA anti-tTG antibody followed by duodenal biopsy in serology-positive patients.
Results:
Out of a total of 464 patients, group A constituted 382 patients, CLD related to ethanol (155), cCLD (147), hepatitis B (42), hepatitis C (21), autoimmune (10), and BCS (7), whereas 82 patients were in group B with NCPF (64) and EHPVO (18). Total 29 patients were diagnosed with CD in both groups, 17 in group A (4.5%) and 12 in group B (14.6%). In group A, 13 patients with cCLD, two with HBV-related CLD, one with BCS, and one with autoimmune-related CLD were concomitantly diagnosed as CD. In group B, CD was diagnosed in 12 patients of NCPF (11) and EHPVO (1). Liver histology showed chronic hepatitis in two patients and was normal in three patients.
Conclusion:
CD is common in PHT of different etiology, especially in cCLD, NCPH and autoimmune hepatitis; however, the etiological basis for this association is still to be defined. The likelihood of CD is higher in liver disease than the general population, and these patients should be screened for CD.
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